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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72663생성일: 2026년 10월 25일

Acetic Anhydride → (E)-3-methoxy-2-nitro-6-((2,4,6-trimethoxystyrylsulfonyl)methyl)pyridine

https://huagongshe.com/reaction/72663

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물2,4,6-TrimethoxybenzaldehydeHCID 70019—
반응물HCID 67994551HCID 67994551—
용매TolueneHCID 1140—
생성물(E)-3-methoxy-2-nitro-6-((2,4,6-trimethoxystyrylsulfonyl)methyl)pyridineHCID 8669090635.3%

반응 단계

A mixture of 2-((5-methoxy-6-nitropyridin-2-yl)methylsulfonyl)acetic acid (0.29 g, 1.0 mmol) in dry toluene (2 mL) was added 2,4,6-trimethoxybenz-aldehyde (0.196 g, 1.0 mmol) and acetic anhydride (0.38 mL). After refluxing for 5 hrs, the reaction mixture was evaporated to dryness. The residue was precipitated by adding methanol (15 mL). The precipitate was filtered to give 150 mg (35%) the titled compound as grey coloured powder. 1H-NMR (Acetone-D6): δ 3.92 (s, 9H, 3×OCH3), 4.07 (s, 3H, OCH3), 4.52 (s, 2H, CH2), 6.32 (s, 2H, Ph-H), 7.20 (d, J=15.6 Hz, 1H, CH), 7.74 (d, 1H, J=15.6 Hz, CH), 7.87 (d, 1H, J=8.4 Hz, Py-H), 7.95 (d, 1H, J=8.8 Hz, Py-H); HR-MS (ESI+) m/z 425.1053 [M+1]+ C18H20N2O8S requires 424.0940.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829003B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-e8c7e36a8cd9498bb2743f95ead1cd29
출처 메모uspto-grants-2014_09